Canonical Allele Identifier: CA1931513329

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845364C= , CM000672.2:g.99845364C=	GRCh38
NC_000010.10:g.101605121C= , CM000672.1:g.101605121C=	GRCh37
NC_000010.9:g.101595111C=	NCBI36
NG_011798.1:g.67659C=
NG_011798.2:g.67767C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3988-260C= MANE Select	ENSP00000497274.1:n.3988-260C=
ENST00000649459.1:n.336-260C=
ENST00000370449.8:c.3988-260C=	ENSP00000359478.4:n.3988-260C=
NM_000392.4:c.3988-260C=	NP_000383.1:n.3988-260C=
XM_006717630.2:c.3292-260C=	XP_006717693.1:n.3292-260C=
XR_945604.1:n.4177-319C=
XR_945605.1:n.4052-260C=
NM_000392.5:c.3988-260C= MANE Select	NP_000383.2:n.3988-260C=
XM_006717630.3:c.3292-260C=	XP_006717693.1:n.3292-260C=
XR_945604.3:n.4231-319C=
XR_945605.3:n.4104-260C=